Offerings
Uses
The Race
About Us
Resources
Create a CKB Account
Create a mastermind account

Clinical Diagnostics

Accelerate NGS variant interpretation with rapid search and insight into the full text of the genomic literature

Clinical Uses

Precision Therapeutics

Partner with us to gain a comprehensive view of the genetics of your disease of interest, from discovery to commercialization

Pharma Uses

Software Solutions

Explore our platforms for germline and somatic variant interpretation


Access article information on more than 26 million variants, as well as curated germline variant content.

Meet Mastermind

Our Cancer Knowledgebase is used to interpret cancer variants, connecting them to therapies and clinical trials


Meet CKB

Services

Partner with our team of experts to create Tailored Solutions for your unique needs

Clinical Diagnostic Services
Precision Therapeutics Services

Data

Gain access to an expansive, constantly updated database of curated genomic information

Learn More
Offerings
Software
Clinical Diagnostics Services
Precision Therapeutics Services
Data
Somatic Knowledgebase
Uses
The Race
About Us
Resources
schedule a discovery call
Create a mastermind account
Create a CKB Account
< Resources

Download

Mastermind Variant Interpretation Poster

‍

Use the Mastermind Variant Interpretation Poster to learn the ACMG Variant Interpretation framework and organize your variant interpretation activities

‍

Submit this form to download the poster:

‍

File Details

Your PDF download is a high resolution print-ready file that measures 18” high x 24” wide (horizontal orientation). Save and send this file to your trusted printing source to display in your lab, classroom, or workspace.

‍

Download PDF
The World’s Most Comprehensive Source of Genomic Evidence

Mastermind accelerates variant interpretation with immediate insight into the full text of millions of scientific articles. Prioritize your search results by clinical relevance and find what you are looking for 5-10 times faster

Create your free account
The Most Comprehensive Source of Curated Genomic Evidence + Scientific Experts

We help provide insights into key genetic drivers of diseases and relevant biomarkers. By working together to understand this data, we enable scientists and researchers to make more informed decisions on programs of interest. To learn more about how we can partner together to find your genomic variant solutions, we invite you to click on the link below.

Contact Us
Offerings
SoftwarePrecision Therapeutics ServicesClinical Diagnostic ServicesData Access
Uses
Clinical UsesPharmaceutical Uses
The Race
About Us
Resources
Careers
News, Press & Events
Investors
Contact Us
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
Citing MastermindTerms & ConditionsPrivacy PolicyCopyright © 2024 Genomenon, Inc. All rights reserved.

By using this website, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts. View our Privacy Policy for more information.

Accept